Valve for dilator and sheath assembly

ABSTRACT

A sheath assembly includes an elongated hollow sheath body having a proximal body end, a distal body end, and a longitudinal axis extending between the proximal body end and the distal body end. A sheath hub is fixedly connected to the proximal body end and includes a hub proximal end and a hub distal end with a through passage extending from the hub distal end to the hub proximal end and in communication with the hollow sheath body. The sheath hub further defining a valve seat proximate the hub proximal end. A valve is seated in the valve seat and includes a valve body with a bisecting slot extending into a proximal surface of the valve body and terminating at a depth less than the thickness of the valve body such that the remaining portion of the valve body distally of the slot defines a bridge extending between opposed halves of the valve body such that a distal surface of the valve body is substantially continuous, the valve extending across and sealing the through passage.

This application claims the benefit of U.S. Provisional Appln. No.61/648,132 filed on May 17, 2012 and U.S. Provisional Appln. No.61/725,509 filed on Nov. 13, 2012, both of which are incorporated hereinby reference.

FIELD OF THE INVENTION

This invention relates to invasive medical devices which aid in thecatheterization of human blood vessels. In particular, this inventionrelates to a releasably locking dilator and tear away sheath assembly,which is used to enlarge an opening in a patient's blood vessel duringinsertion of a catheter into the blood vessel and then guide thecatheter into the blood vessel to be catheterized.

BACKGROUND OF THE INVENTION

Catheters are used in numerous medical procedures. In particular,catheters are used for the introduction or removal of fluids fromvarious venous regions and vessels throughout the body, such as forhemodialysis. The procedure by which these catheters are introduced tothe body is delicate and complex. One particularly intricate challengeto catheterization is enlarging a hole in the flesh and vessel to becatheterized while minimizing blood loss and trauma to the patient.

Generally, to insert any catheter in a blood vessel, the vessel isidentified by aspiration with a long hollow needle in accordance withthe Seldinger technique. When blood enters a syringe attached to theneedle, indicating that the vessel has been found, a thin guide wire isthen introduced, typically through the syringe needle or otherintroducer device, into the interior of the vessel. The introducerdevice is then removed, leaving the guide wire within the vessel. Theguide wire projects beyond the surface of the skin.

At this point, several options are available to a physician for catheterplacement. The simplest option is to pass a catheter into the vesseldirectly over the guide wire. The guide wire is then removed. However,use of this technique is only possible in cases where the catheter is ofa relatively small diameter, made of a stiff material and notsignificantly larger than the guide wire. If, however, the catheter isof a relatively large diameter and/or made of a soft material, onepreferable method of inserting the catheter into the vessel is throughan introducer sheath. The introducer sheath is simply a large, stiff,thin-walled tube, which serves as a temporary conduit for the catheterthat is being placed. The sheath is positioned by placing a dilator,which has a hollow passageway along its longitudinal axis, inside of thesheath and passing both the dilator and the sheath together into thevessel over the guide wire. The dilator expands the opening in the bloodvessel to allow for catheter insertion into the vessel. The guide wireand dilator are then removed, leaving the thin-walled sheath in place.The catheter is then inserted into the vessel through the sheath.

In a setting where a catheter with a hub or other attachment at theproximal end of the catheter has a feature which is larger than that ofthe inner diameter of the sheath, it is necessary to have a tear-awaysheath that can be split away from the catheter as the sheath is beingremoved from the patient. By splitting the sheath along its longitudinalaxis as the sheath is being removed from the patient, the insertingphysician will be able to pull out the sheath in such a way that theportion removed from the patient is split, thereby not interfering withany encumbrances on the catheter. Generally, tear away sheaths aremanufactured in a way that aids in the tearing of the sheath at twoopposing points on the circumference of the sheath, thereby splittingthe sheath into two halves separated longitudinally through the centerof the sheath.

A sheath is generally constructed with a hub at its proximal end. Thishub serves as a handle, a mating point for a dilator, and a flat surfaceto aid in the prevention of blood loss or contamination. When a sheathneeds to be split apart in order to be successfully withdrawn from thebody while leaving the catheter in place, the hub will also have to besplit apart in order to clear the catheter. Preferably, the hub willsplit along the same lines as the sheath. To accomplish this, the hubmust be designed with reveals or other weaknesses along two longitudinallines aligned with the weaknesses in the sheath. Some previous examplesof these weaknesses are tabs or webs which connect two halves of thehub, or recesses in the material comprising the hub. The weaknesses inthe hub will help the inserting physician to break apart the hub in linewith the tear seams on the sheath.

Another important facet of the hub is a set of tabs that protrude fromthe center. These tabs not only help the inserting physician to align,insert and withdraw the sheath, but also to pull the sheath so that thesheath can be removed from around a catheter while still leaving thecatheter in place. There are a number of different tab configurations,but it is important to have one which allows for easy maneuverability,control, and leverage. One design includes a hub wherein the tabsprotrude from the hub perpendicular to a plane which includes the tearseams in the sheath and the longitudinal axis of the sheath. In thisdesign, the tabs are diametrically opposed from each other and arespaced in such a way that when the tabs are grasped and pulled apartfrom each other, the sheath and its hub will split down the middle.Another desirable feature of the tabs is that the tabs provide leveragefor breaking apart the hub in a manner that does not cause trauma to theincision in the body.

During insertion, especially in the time between the removal of thedilator from the sheath and the insertion of the catheter through thesheath, it is possible for blood loss through the sheath, or theintroduction of contaminants or air through the sheath and into thevessel. For this reason, it is desirable that measures be taken toprevent blood, air or contaminants from traveling through the sheath. Inthe past, inserting physicians have simply held their thumb over theopening in the proximal end of the sheath; however, a more permanent andreliable means for preventing blood, air or contaminants from travelingthrough the sheath is desirable. It is therefore desirable for the hubto include a valve located in the sheath. Such a valve would facilitatethe insertion of objects such as a catheter or dilator through thesheath while restricting blood loss and reducing the chance ofcontaminants entering the patient's bloodstream when the sheath is notengaged with a dilator or a catheter.

The dilator has a long tubular section, the outside diameter of which isslightly smaller than the inside diameter of the sheath. The dilatoralso has a pointed tip on its distal end and a hollow center, which runsalong the entire length of the dilator. The dilator is inserted into thebody with the guidewire running through its center, thereby allowing thetip of the dilator to follow the guidewire to the place that is to becatheterized. On its proximal end, the dilator may have a hub. Like thehub of the sheath, this hub can also serve a number of purposes, such asproviding a stable handle to aid in guiding the dilator into the vein,and as a mechanism which can mate with the sheath hub to form a lockedconnection.

Some dilator and sheath assemblies that include a connection between thedilator and sheath are known. U.S. Pat. No. 5,885,217 to Gisselberg etal. discloses a dilator and sheath assembly, wherein the dilator andsheath are held together by locking tabs which provide a stop to holdthe dilator in place during insertion. However, in this configuration,the dilator may rotate about its longitudinal axis in relation to thesheath, thereby inadvertently and prematurely disengaging the dilatorfrom the sheath. U.S. Pat. No. 5,098,392 to Fleischhacker et al.discloses a dilator and sheath assembly, wherein the dilator is attachedto the sheath through a clamp wherein the clamp is part of the dilatorhub. However, this design presents the ability to come unclamped leadingto the dilator backing out of the sheath. U.S. Pat. No. 4,772,266 toGroshong discloses a dilator and sheath assembly, wherein the hubs ofthe dilator and the sheath lock together by means of compression.However, it would be possible for the dilator to back out of the sheathin this configuration if excessive force is exerted on the tip of thedilator.

It would be beneficial to provide a dilator and sheath assembly thatincorporates a stable releasably locking mechanism to prevent thedilator from backing out of the sheath longitudinally during insertionwhich is not prone to coming unlocked or releasing during use. It wouldalso be beneficial for the sheath of the dilator and sheath assembly tohave a means for sealing the passageway to the patient's vessel, therebyrestricting blood loss and reducing the introduction of contaminantsinto the bloodstream.

SUMMARY OF THE INVENTION

Briefly, the present invention provides a releasably locking dilator andsheath assembly and methods for releasing the dilator from the sheathand longitudinally splitting the sheath in the course of inserting acatheter into a desired vessel to be catheterized.

In one aspect, the invention provides a valve for sealing the hub of asheath assembly, the valve comprising a valve body with a bisecting slotextending into a proximal surface of the valve body and terminating at adepth less than the thickness of the valve body such that the remainingportion of the valve body distally of the slot defines a bridgeextending between opposed halves of the valve body such that a distalsurface of the valve body is substantially continuous.

In another aspect, the invention provides a sheath assembly including anelongated hollow sheath body having a proximal body end, a distal bodyend, and a longitudinal axis extending between the proximal body end andthe distal body end. A sheath hub is fixedly connected to the proximalbody end and includes a hub proximal end and a hub distal end with athrough passage extending from the hub distal end to the hub proximalend and in communication with the hollow sheath body. The sheath hubfurther defining a valve seat proximate the hub proximal end. A valve isseated in the valve seat and includes a valve body with a bisecting slotextending into a proximal surface of the valve body and terminating at adepth less than the thickness of the valve body such that the remainingportion of the valve body distally of the slot defines a bridgeextending between opposed halves of the valve body such that a distalsurface of the valve body is substantially continuous, the valveextending across and sealing the through passage.

In a further aspect, the sheath body of the sheath assembly includes atleast one tear seam extending in a plane between the proximal body endand the distal body end and the sheath hub includes at least onelongitudinal notch, and the at least one tear seam, the at least onelongitudinal notch and the bisecting slot are co-planar.

In another aspect, the invention provides a dilator and sheath assembly.The dilator includes an elongated dilator stem having a proximal dilatorend and a dilator hub fixedly connected to the proximal dilator end,wherein the dilator hub includes a locking portion at a distal portionthereof. The sheath assembly includes an elongated tubular portionhaving a proximal sheath end, a distal sheath end, and a longitudinalaxis extending between the proximal sheath end and the distal sheathend, wherein the tubular portion is sized to receive the dilator stemand includes at least one tear seam extending in a plane between theproximal sheath end and the distal sheath end. A sheath hub is fixedlyconnected to the proximal sheath end. A valve is assembled to the sheathhub proximal of the proximal sheath end and at least one cap member issecured to the sheath hub proximal portion. The at least one cap memberdefines a mating locking portion wherein the locking portion of thedilator hub and the mating locking portion of the cap provide areleasably locking engagement between the dilator and the sheath.

BRIEF DESCRIPTION OF THE DRAWINGS

The accompanying drawings, which are incorporated herein and constitutepart of this specification, illustrate the presently preferredembodiments of the invention, and, together with the general descriptiongiven above and the detailed description given below, serve to explainthe features of the invention. In the drawings:

FIG. 1 is a perspective view of a releasably locking dilator and sheathassembly in a locked state in accordance with an embodiment of thepresent invention.

FIG. 2 is an exploded perspective view of the assembly of FIG. 1.

FIG. 3 is a perspective view of an exemplary dilator hub in accordancewith an embodiment of the invention.

FIG. 4 is a cross-sectional view along the line 4-4 in FIG. 3.

FIG. 5 is a top perspective view of an exemplary sheath hub inaccordance with an embodiment of the invention.

FIG. 6 is a bottom perspective view of the exemplary sheath hub of FIG.5.

FIG. 7 is a cross-sectional view along the line 7-7 in FIG. 5.

FIG. 8 is a top perspective view of an exemplary valve in accordancewith an embodiment of the invention.

FIG. 9 is a bottom perspective view of the exemplary valve of FIG. 8.

FIG. 10 is a top plan view of the exemplary valve of FIG. 8.

FIG. 11 is a cross-sectional view along the line 11-11 in FIG. 10.

FIG. 12 is a cross-sectional view along the line 12-12 in FIG. 10.

FIG. 13 is a perspective view of another exemplary valve in accordancewith an embodiment of the invention.

FIG. 14 is a top perspective view of the exemplary valve of FIG. 13.

FIG. 15 is a bottom perspective view of the exemplary valve of FIG. 13.

FIG. 16 is a side elevation view of the exemplary valve of FIG. 13.

FIG. 17 is a cross-sectional view along the line 17-17 in FIG. 13.

FIG. 18 is a cross-sectional view along the line 18-18 in FIG. 13.

FIG. 19 is an expanded view of a portion of the valve of FIG. 18.

FIG. 20 is a top perspective view of another exemplary valve inaccordance with an embodiment of the invention.

FIG. 21 is a side elevation view of the exemplary valve of FIG. 20.

FIG. 22 is a cross-sectional view along the line 22-22 in FIG. 20.

FIG. 23 is a bottom perspective view of the exemplary valve of FIG. 20.

FIG. 24 is a cross-sectional view along the line 24-24 in FIG. 23.

FIG. 25 is a front perspective view of an exemplary cap member inaccordance with an embodiment of the invention.

FIG. 26 is a rear perspective view of the exemplary cap member of FIG.25.

FIG. 27 is a perspective view of the exemplary hub assembly in anassembled condition with the sheath omitted.

FIG. 28 is a perspective cross-sectional view along the line 28-28 inFIG. 27.

FIG. 29 is a planar view of the cross-sectional view of FIG. 28.

FIG. 30 is a cross-sectional view along the line 30-30 in FIG. 27.

FIGS. 31-33 are perspective views of the releasably locking dilator andthe sheath assembly sequentially illustrating positioning and locking ofthe dilator relative to the sheath assembly.

DETAILED DESCRIPTION OF THE INVENTION

In the drawings, like numerals indicate like elements throughout.Certain terminology is used herein for convenience only and is not to betaken as a limitation on the present invention. The terms “distal” and“proximal” refer to the directions “away from” and “closer to,”respectively, the body of the physician inserting the dilator and sheathassembly into a patient. As used herein, the term “slot” refers to aseparation of material of a body which extends only partially throughthe body and does not exit out an opposite surface of the body and theterm “slit” refers to a separation of material of a body which passesthrough the body from one surface out the other surface. The terminologyincludes the words above specifically mentioned, derivatives thereof,and words of similar import. The following describes a preferredembodiment of the present invention. However, it should be understood,based on this disclosure, that the invention is not limited by thepreferred embodiment described herein.

Referring to FIGS. 1 and 2, an exemplary embodiment of a releasablylocking dilator and sheath assembly 10 is shown. The assembly 10generally includes a dilator 20 and a sheath assembly 40, which arereleasably lockable to each other. The dilator 20 is longer than thesheath assembly 40 so that the dilator 20, in the releasably lockedposition as shown in FIG. 1, passes through the sheath assembly 40 sothat a distal tip 37 of the dilator 20 extends beyond the distal end 46of the sheath assembly 40.

Referring to FIGS. 1-4, the dilator 20 is an elongated device thatincludes a proximal end 21, a distal end 35 with a stem 36 and dilatorhub 22 extending between the proximal end 21 and the distal end 35. Atthe distal end 35 of the dilator stem 36, a transition portion 38reduces in diameter to a conically shaped, open distal tip 37. When in areleasably connected state with the dilator 20 inside of the sheathassembly 40, the dilator 20 and sheath assembly 40 share the samelongitudinal axis “L”. The exterior diameter of the stem 36 of thedilator 20 is sized to allow a slight frictional engagement between theinside of the distal end 46 of the sheath body 44 and the outside of thedilator stem 36. This frictional engagement serves to form a sealbetween the dilator 20 and the sheath assembly 40 and reduce or preventblood seepage through the sheath assembly 40 while the dilator 20 isreleasably connected thereto. Preferably, the dilator 20 includes ahollow passageway 30 along the length of the dilator 20 from the distaltip 37 to the proximal end of the dilator hub 22. The hollow passageway30 allows the dilator 20 to be inserted over a guidewire (not shown) andfollow the guidewire to the desired position inside the vessel to becatheterized.

The proximal end 21 of the dilator 20 comprises a dilator hub 22 fixedlyconnected to the dilator stem 36 such as by an adhesive, ultrasonicbonding, insert molding or another method known to those skilled in theart. The dilator hub 22 includes a body 24 extending between a proximalend 26 and a distal end 28. The proximal end 26 includes a connector 27,for example, the male portion of a luer connector. The connector 27 maybe used as a temporary fitting for any apparatus (not shown) that may berequired to be attached to the dilator 20. The distal end 28 of thedilator hub 22 includes a connector ring 29 configured to receive aproximal end of the stem 36 whereat the stem 36 is fixedly connected tothe hub 22. Alternatively, the ring 29 may be received within the stem36 and fixedly connected.

A locking portion 39 extends from the hub body 24 adjacent to the distalend 28 of the hub 22. The locking portion 39 of the present embodimentincludes an elongate platform 32 extending radially from the hub body24. The platform 32 preferably has a length larger than its width suchthat the platform 32 extends from opposed sides of the hub body 24. Anextension portion 33 extends from each end of the platform 32, extendingsubstantially parallel to the axis L. An engagement portion 34 extendsperpendicularly from each extension portion 33 substantially parallel tothe platform 32 such that locking grooves 45 are defined on oppositesides of the hub body 24. The inside surfaces of the extension portions33 are spaced from one another a distance F while the engagementportions 34 are spaced from one another by a distance E. Preferably, astop member 25 depends from each side edge of the platform 32. Thelocking portion 39 is configured to engage a portion of the sheathassembly 40 to lock the dilator 20 relative thereto, as will bedescribed in more detail hereinafter.

Referring to FIGS. 1 and 2, the sheath assembly 40 is used to aid in theinsertion of a catheter (not shown) into a vessel (not shown) to becatheterized, as is well known in the art. Since the sheath assembly 40includes a sheath body 44 which is generally more rigid than a catheter,the sheath assembly 40 can be maneuvered into place with less effort andtrauma to the patient than a catheter. The catheter is then insertedinto the vessel through the sheath assembly 40. Once the catheter is inplace, the sheath assembly 40 may be removed, thereby leaving thecatheter in its desired position. If the sheath assembly 40 has anyencumbrance, such as a hub, on its proximal end, the sheath assembly 40will have to be split in order to remove it from the patient's bodywhile leaving the catheter in place.

In the present embodiment, the sheath assembly 40 extends between aproximal end 41 and a distal end 43 and includes a sheath body 44, asheath hub 50, a valve 80 and cap members 100. A through passage 42extends through the sheath body 44 and sheath hub 50 from the distal end43 to the proximal end 41. The through passage 42 is sealed by the valve80 as described in more detail hereinafter.

The sheath body 44 is a hollow tubular member which preferably has atapered distal end 46. At least one tear seam 48 is longitudinallydisposed along the entire length of the sheath body 44. In thispreferred embodiment, two tear seams 48 are present. The tear seams 48are located on opposite sides of the sheath body 44 such that a planeextending through the two tear seams 48 bisects the sheath body 44longitudinally. Preferably, the plane contains the longitudinal axis L.The proximal end of the sheath body 44 is fixedly connected to thedistal end of the sheath hub 50.

Referring to FIGS. 5-7, the sheath hub 50 includes a conical body 52which tapers from a wider proximal end 51 to a narrower distal end 53.Two diametrically opposed notches 54 are defined longitudinally alongthe hub body 52 from the distal end 53 to the proximal end 51. At theradial inner end of each notch 54, a bridge 55 extends between the twoopposed halves 52 a, 52 b of the body 52. The hub body 52 is preferablymolded as a unitary component with the bridges 55 extending between thehalves 52 a, 52 b and the notches 54 preformed, however, the hub body 52may be otherwise formed. For example, the body halves 52 a, 52 b may beformed as separate components which are joined by the bridges 55 afterformation. Alternatively, the body 52 may be formed as a unitarystructure without any notches and the notches are formed through a postmolding process, leaving just the bridges 55 extending between thehalves 52 a, 52 b. While continuous bridges 55 are illustrated, theinvention is not limited to such and other structures, including thosedescribed in U.S. Pat. Nos. 6,796,991, 7,422,571 and 8,052,646, each ofwhich is incorporated herein by reference, may be utilized to join theopposed halves 52 a, 52 b with a weakened tear line definedtherebetween. Each notch 54 is preferably aligned with one of the tearseams 48 of the sheath body 44 such that the notches 54 and the tearseams 48 of the sheath body 44 are coplanar.

Referring to FIG. 7, the interior surface of the hub body 52 at thedistal end defines a conical surface 56 configured to receive andfixedly connect the sheath body 44 proximal end. The sheath hub 50 isfixedly connected to the proximal end of the sheath body 44 such as byan adhesive, ultrasonic bonding, insert molding or any other methodknown to those skilled in the art. The diameter of this conical surface56 may be manufactured to different sizes to allow the hub 50 to be usedwith larger or smaller size sheath bodies 44. Alternatively, the conicalsurface 56 may be manufactured to a standard size and a spacer ring (notshown) may be positioned between the sheath body 44 and the conicalsurface 56 to sealingly close the distal end of the hub body 52.

The interior surface of the hub body 52 tapers outwardly from theconical surface 56 to an annular valve seat 60 which extends about thethrough passage 42. The proximal end 51 of the hub body 52 defines anannular wall 58 about the valve seat 60. The valve seat 60 includes aplanar surface 62 extending about the through passage 42. The planarsurface 62 is preferably continuous about the entire circumference ofthe through passage 42 such that it defines a continuous sealingsurface. An annular groove 63 is defined between the planar surface 62and the annular wall 58. A plurality of alignment posts 64 extendproximally from within the groove 63 and are configured properly alignthe valve 80 received within the valve seat 60 as described in moredetail below.

A plurality of retaining tabs 57 extend radially outward from the outersurface of the wall 58 for securing the cap members 100 as describedbelow. Each retaining tab 57 preferably tapers outwardly moving from theproximal end to the distal end.

First and second diametrically opposed winged tabs 70 extend from thesheath hub body 52 adjacent its proximal end 51. The tabs 70 arecircumferentially offset 90° relative to the notches 54. In theillustrated embodiment, the first and second tabs 70 each include aperpendicular portion 72, perpendicular to the longitudinal axis L andan angled portion 74. A brace member 76 may extend between eachperpendicular portion 72 and a distal portion of the hub body 52. Inaddition to supporting the perpendicular portions 72, the braces 76 alsohelp to concentrate the forces as the sheath hub 50 is torn away in aknown manner. As shown in FIG. 6, an angle α extends between theproximal surface of the perpendicular portion 72 and the angled portion74 of each of the wings 42. The angle α ranges from approximately 90° toapproximately 179°. Preferably, the angle α is between approximately130° to approximately 140°; however, those skilled in the art willrecognize that the angle α can have other ranges as well. The angledportions 74 of the winged tabs 70 include raised ridges 75 on theirproximal and distal surfaces to aid in gripping the tabs 70.Alternatively, other raised features on the winged tabs 70, such asbumps or a crosshatched pattern (not shown) may also assist the grippingthe winged tabs 70.

The sheath body 44 is preferably constructed of high-densitypolyethylene, low-density polyethylene or polytetrafluoroethylene. Thesheath hub 50 is preferably constructed of high-density polyethylene orpolypropylene. The dilator stem 26 is preferably constructed ofhigh-density polyethylene, low-density polyethylene or polypropylene.The dilator hub 22 is preferably constructed of high-densitypolyethylene or polypropylene.

Referring to FIGS. 8-12, an exemplary valve 80 will be described. Thevalve 80 has a cylindrical body 82 with a diameter substantially equalto or slightly larger than the inside diameter of the hub body annularwall 58. While the valve body 82 is shown as cylindrical, it may haveany other shape which complements the shape of the valve seat 60 andannular wall 58. The body 82 extends between a proximal surface 86 and adistal surface 94. A bisecting slot 83 extends into the proximal surface86 across the body 82 through the center thereof such that the body 82includes opposed body halves 82 a and 82 b. The slot 83 terminates priorto the distal surface 94 such that the body halves 82 a and 82 b arejoined by a bridging portion 84 along the distal surface 94. Thebridging portion 84 has a reduced thickness t relative to the totalthickness T of the valve body 82. Preferably, the thickness t of thebridging portion is between approximately 0.002 to 0.006 inches and morepreferably between approximately 0.003 to 0.004 inches. For relativecomparison, the valve body thickness may be about 0.1 inches. With thisconfiguration, the bridging portion 84 retains the body halves 82 a, 82b together prior to assembly and acts to seal the through passage 42,but remains easily split as an instrument is passed through the valve 80and easily separated when the sheath assembly 40 is split.

The valve body 82 is preferably molded as a unitary component with thebridge portion 84 extending between the halves 82 a, 82 b and the slot83 preformed, however, the valve body 82 may be otherwise formed. Forexample, the body halves 82 a, 82 b may be formed as separate componentswhich are joined by the bridge portion 84 after formation.Alternatively, the body 82 may be formed as a unitary structure and theslot is formed through a post molding process, for example, cutting,leaving just the bridge portion 84 extending between the halves 82 a, 82b. Preferably, the valve 80 is constructed of silicone, however, thoseskilled in the art will recognize that the valve 80 may be constructedout of any material that is sufficiently resilient to accommodate theobjects inserted therethrough and return to a closed position. Thematerial preferably has a durometer between 10 A to 40 A. The width G ofthe slot 83 is preferably minimal and is generally dictated by themethod of manufacture. In the present embodiment, the width G ispreferably about 0.005 inches, however, the width G may approach zero,as in simple separation of material, or may be larger than 0.005 inches.For example, if the slot 83 is formed through a post molding cuttingoperation, the width G may approach zero. Alternatively, the halves 82a, 82 b may be molded at an angle to one another with the bridge portion84 extending therebween and the width G relatively large. As the halves82 a, 82 b are pivoted toward one another into a common plane, the widthG may approach zero.

The proximal surface 86 defines an outer annular planar portion 87 thatis substantially perpendicular to the longitudinal axis L when the valveis assembled within the sheath hub 50 (see FIGS. 29 and 30). An annulargroove 88 is defined along the planar portion 87 and is configured toreceive a retaining ridge 116 of the cap members 100 and alsofacilitates hinging of a center portion of the valve body 82 as an itemis passed through the valve 80, as described in more detail below. Aplurality of alignment holes 98 extend from the distal surface 94 to theproximal surface 86 are defined circumferentially spaced about theplanar portion 87. While the alignment holes 98 are illustratedextending completely through the body 82, such is not required.Alternatively, the alignment holes 98 may be formed as blind holesopening at the distal surface 94.

The alignment holes 98 are configured to receive respective ones of thealignment posts 64 of the valve seat 60. As seen in FIG. 10, thealignment holes 98 are positioned in a non-symmetrical configuration.The alignment posts 64 are arranged in a corresponding configuration. Assuch, the valve 80 can only be positioned in the sheath hub 50 in aproper orientation with the proximal surface 86 facing proximally andthe slot 83 co-planar with the notches 54.

Radially inward of the planar portion 87, the proximal surface 86defines a conical portion 89 which tapers to a central blind bore 90.The bore 90 terminates in a bottom surface 91 that is spaced from thebody distal surface 94 such that the bore 90 does not pass completelythrough the valve body 82. The bore 90 may be formed with a narrowingtaper from the entrance at the conical portion 89 to the bottom surface91. The conical portion 89 and the bore 90 serve to guide a guidewire(not shown), the dilator distal tip 37, the catheter tip (not shown), orany other instrument as they are respectively passed through the valve80. The bore 90 has a diameter d which is relatively small compared tothe diameter D of the valve body 82. The bore diameter d is generallyrelated to the diameter of an intended guide wire and may be in therange of approximately 0.03 to 0.2 inches. For relative comparison, thediameter of the valve body D may be in the range of approximately 0.4 to0.8 inches. As shown in FIG. 12, the slot 83 may extend deeper than thebore 90 such that the bottom surface 91 is proximally spaced from theproximal surface of the bridge portion 84.

Optionally, a pilot hole 92 extends through the bridge portion 84 andexits out the body distal surface 94. The pilot hole 92 is preferablyco-axial with the bore 90. The guide hole 92 has a minimal diameter, forexample, about or smaller than the diameter of a guidewire, and servesto provide a propagation point to split the bridge portion 84 and allowpassage of an instrument through the valve 80. In normal assembly asdescribed below, the dilator 20 will be the first instrument passedthrough the valve 80. The dilator distal tip 37 will be guided to thepilot hole 92 by the conical surface 89 and the bore 90. As the distaltip 37 reaches the pilot hole 92, it will pierce the bridge portion 84,with the bridge portion 84 splitting outwardly from the pilot hole 92.As the dilator stem 20 passes, the resiliency of the valve 80 will causethe valve 80 to seal against the stem 20 as it extends therethrough. Thevalve 80 will function in a similar manner as a catheter or otherinstrument is passed through the valve 80. In each case, which everinstrument is passed through the valve 80, the bridge 84 will slit onlyenough to pass the particular device and will effectively create acustom passage sized just to the device passing through. As the dilator20 or other instrument is removed, the resiliency of the valve 80 willcause the valve 80 to substantially seal upon itself.

Referring to FIGS. 9 and 12, the distal surface 94 of the valve body 82includes a pair of opposed arcuate grooves 96. Each groove 96 extendsslightly less than 180° such that the grooves 96 are separated byopposed non-grooved portions 95 of the distal surface 94. Thenon-grooved portions 95 are preferably co-planar with the slot 83. Thegrooves 96 in conjunction with the non-grooved portions 95 provide aresilient hinge effect for the valve 80. As an instrument or the like ispassed through the valve 80, the central portion of the valve body 82will begin to deflect distally over an arcuate path as indicated byarrows A in FIG. 12. The grooves 96 provide space for the proximateportions 97 of the distal surface 94 to move during such deflection toallow easier passage, while the non-grooved portions 95 provide somerigidity and assist in restoring the valve central portion to itoriginal position as the instrument is removed.

Referring to FIGS. 13-19, another exemplary valve 80′ will be described.The valve 80′ is similar to the prior embodiment and has a cylindricalbody 82′ with a diameter substantially equal to or slightly larger thanthe inside diameter of the hub body annular wall 58. While the valvebody 82′ is shown as cylindrical, it may have any other shape whichcomplements the shape of the valve seat 60 and annular wall 58. The body82′ extends between a proximal surface 86′ and a distal surface 94′. Abisecting slot 83′ extends into the proximal surface 86′ across the body82′ through the center thereof such that the body 82′ includes opposedbody halves 82 a′ and 82 b′. The slot 83′ terminates prior to the distalsurface 94′ such that the body halves 82 a′ and 82 b′ are joined by abridging portion 84′ along the distal surface 94′. The bridging portion84′ has a reduced thickness t1 and t2 relative to the total thickness Tof the primary valve body 82′, i.e. excluding the thickness of theconvex portion 99′. In the present embodiment, the bridge portion 84′has varying thicknesses t1 and t2, with the central thickness t1 beinglarger than the thickness t2, however, the bridge portion 84′ may have aconstant thickness, for example, equal to t2. Preferably, the thicknesst2 of the outer bridging portion is between approximately 0.003 to 0.012inches and more preferably between approximately 0.005 to 0.009 inches.Preferably, the thickness t1 of the central bridging portion is betweenapproximately 0.003 to 0.012 inches and more preferably is betweenapproximately 0.005 to 0.009 inches. For relative comparison, the valvebody thickness may be about 0.1 inches. With this configuration, thebridging portion 84′ retains the body halves 82 a′, 82 b′ together priorto assembly and acts to seal the through passage 42.

In the present embodiment, the valve body 82′ is preferably molded as aunitary component and the slot 83′ is formed through a post moldingprocess, for example, cutting, leaving just the bridge portion 84′extending between the halves 82 a′, 82 b′, however, the valve body 82′may be otherwise formed. For example, the body halves 82 a′, 82 b′ maybe formed as separate components which are joined by the bridge portion84′ after formation or the halves 82 a′ and 82 b′ may be molded with aslot therebetween and just the bridge 84′ extending therebetween.Preferably, the valve 80′ is constructed of silicone, however, thoseskilled in the art will recognize that the valve 80′ may be constructedout of any material that is sufficiently resilient to accommodate theobjects inserted therethrough and return to a closed position. Thematerial preferably has a durometer between 10 A to 40 A. In thepresently illustrated embodiment wherein the slot 83′ is created by postmold scoring, the width G of the slot 83′ approaches zero as thematerial of the halves 82 a′, 82 b′ comes back together.

The proximal surface 86′ defines an outer annular planar portion 87′that is substantially perpendicular to the longitudinal axis L when thevalve is assembled within the sheath hub 50. An annular groove 88′ isdefined along the planar portion 87′ and is configured to receive aretaining ridge 116 of the cap members 100 and also facilitates hingingof a center portion of the valve body 82′ as an item is passed throughthe valve 80′. A plurality of alignment holes 98′ extend from the distalsurface 94′ to the proximal surface 86′ and are definedcircumferentially spaced about the planar portion 87′. While thealignment holes 98′ are illustrated extending completely through thebody 82′, such is not required. Alternatively, the alignment holes 98′may be formed as blind holes opening at the distal surface 94′.

The alignment holes 98′ are configured to receive respective ones of thealignment posts 64 of the valve seat 60. In the present embodiment, thealignment holes 98′ are illustrated in a symmetrical configuration aboutone of the axis of the valve, however, the alignment holes 98′ may bepositioned in a non-symmetrical configuration about all axis as in theprevious embodiment. In either event, the alignment posts 64 arearranged in a corresponding configuration.

Radially inward of the planar portion 87′, the proximal surface 86′defines a conical, concave portion 89′ extending distally. As seen inFIG. 18, the distal surface 94′ defines a convex area 99′ below theconical, concave portion 89′. The bridge 84′ extends across the convexarea 99′. The concave portion 89′ on the proximal surface 86′ and theconvex area 99′ on the distal surface 94′ allow the two sealing faces ofthe body halves 82 a′ and 82 b′ to come back together as the dilator orother medical device is removed.

The present embodiment does not include a bore as in the previousembodiment, but instead includes a bisecting slit 150 that extendsthrough the valve body 82′ from the proximal surface 86′ and out thedistal surface 94′. The bisecting slit 150 is not co-planar with theslot 83′ but instead is at an angle Ω, see FIG. 15, relative to the slot83′. The angle Ω is preferably in a range of approximately 45° to 135°and is most preferably equal to about 90°. In this manner, the sealingfunction of the slit 150 and the splitting function of the slot 83′ areseparated. While a single slit 150 is illustrated, multiple splits atdifferent angles relative to the slot 83′ may be provided.

Referring to FIGS. 18 and 19, it is preferable that the slit 150 is atan angle δ relative to the longitudinal axis L. The angle δ ispreferably in a range of approximately 20° to 70° and is most preferablyequal to about 45°. Preferably the slit 150 is positioned such that theproximal opening 151 of the slit 150 is on one side of the axis L whilethe distal exit 153 is on the opposite side of the axis L.

In normal assembly, the dilator 20 will be the first instrument passedthrough the valve 80′. The dilator distal tip 37 will enter the slit 150and will thereby bypass the bridge portion 84′, without necessitatingsplitting of the bridge portion 84. As the dilator stem 20 passes, theresiliency of the valve 80′ will cause the valve 80′ to seal against thestem 20 as it extends therethrough. The valve 80′ will function in asimilar manner as a catheter or other instrument is passed through thevalve 80′. In each case, which ever instrument is passed through thevalve 80′, the slit 150 will open only enough to pass the particulardevice and will effectively create a general seal about the devicepassing through. As the dilator 20 or other instrument is removed, theresiliency of the valve 80′ will cause the valve 80′ to substantiallyseal upon itself, with the convex configuration of the conical portion89′ assisting in such sealing.

Referring to FIGS. 20-24, another exemplary valve 80″ will be described.The valve 80″ is similar to the prior embodiments and has a cylindricalbody 82″ with a diameter substantially equal to or slightly larger thanthe inside diameter of the hub body annular wall 58. While the valvebody 82″ is shown as cylindrical, it may have any other shape whichcomplements the shape of the valve seat 60 and annular wall 58. The body82″ extends between a proximal surface 86″ and a distal surface 94″. Abisecting slot 83″ extends into the proximal surface 86″ across the body82″ through the center thereof such that the body 82″ includes opposedbody halves 82 a″ and 82 b″. The slot 83″ terminates prior to the distalsurface 94″ such that the body halves 82 a″ and 82 b″ are joined by abridging portion 84″ along the distal surface 94″. The bridging portion84″ has a reduced thickness t relative to the total thickness T of thevalve body 82″. Preferably, the thickness t of the bridging portion isbetween approximately 0.002 to 0.006 inches and more preferably betweenapproximately 0.003 to 0.004 inches. For relative comparison, the valvebody thickness may be about 0.1 inches. With this configuration, thebridging portion 84″ retains the body halves 82 a″, 82 b″ together priorto assembly and acts to seal the through passage 42, but remains easilysplit as an instrument is passed through the valve 80″ and easilyseparated when the sheath assembly 40 is split.

The valve body 82″ is preferably molded as a unitary component with thebridge portion 84″ extending between the halves 82 a″, 82 b″ and theslot 83″ preformed, however, the valve body 82″ may be otherwise formed.For example, the body halves 82 a″, 82 b″ may be formed as separatecomponents which are joined by the bridge portion 84″ after formation.Alternatively, the body 82″ may be formed as a unitary structure and theslot is formed through a post molding process, for example, cutting,leaving just the bridge portion 84″ extending between the halves 82 a″,82 b″. Preferably, the valve 80″ is constructed of silicone, however,those skilled in the art will recognize that the valve 80″ may beconstructed out of any material that is sufficiently resilient toaccommodate the objects inserted therethrough and return to a closedposition. The material preferably has a durometer between 10 A to 40 A.The width G of the slot 83″ is preferably minimal and is generallydictated by the method of manufacture. In the present embodiment, thewidth G is preferably about 0.005 inches, however, the width G mayapproach zero, as explained above, or may be larger than 0.005 inches.

The proximal surface 86″ defines an outer annular planar portion 87″that is substantially perpendicular to the longitudinal axis L when thevalve is assembled within the sheath hub 50. An annular groove 88″ isdefined along the planar portion 87″ and is configured to receive aretaining ridge 116 of the cap members 100 and also facilitates hingingof a center portion of the valve body 82″ as an item is passed throughthe valve 80″. A plurality of alignment holes 98″ extend from the distalsurface 94″ to the proximal surface 86″ are defined circumferentiallyspaced about the planar portion 87″. While the alignment holes 98″ areillustrated extending completely through the body 82″, such is notrequired. Alternatively, the alignment holes 98″ may be formed as blindholes opening at the distal surface 94″.

The alignment holes 98″ are configured to receive respective ones of thealignment posts 64 of the valve seat 60. In the present embodiment, thealignment holes 98″ are illustrated in a symmetrical configuration aboutone of the axis of the valve, however, the alignment holes 98″ may bepositioned in a non-symmetrical configuration about all axis as in theprevious embodiment. In either event, the alignment posts 64 arearranged in a corresponding configuration.

Radially inward of the planar portion 87″, the proximal surface 86″defines a conical, convex portion 89″ extending proximally. As seen inFIG. 22, the distal surface 94″ defines a concave area 99″ below theconical, convex portion 89″. The bridge 84″ extends across the concavearea 99″. The convex portion 89″ on the proximal surface 86″ and theconcave area 99″ on the distal surface 94″ allow the two sealing facesof the body halves 82 a″ and 82 b″ to come back together as the dilatoror other medical device is removed.

The present embodiment does not include a bore as in the firstembodiment, but optionally may include a pilot hole 92″ co-axial withthe valve body 82″. In normal assembly, the dilator 20 will be the firstinstrument passed through the valve 80″. The dilator distal tip 37 willenter the slot 83″ and will pierce the bridge portion 84″, with thebridge portion 84 splitting outwardly from the pilot hole 92″. As thedilator stem 20 passes, the resiliency of the valve 80″ will cause thevalve 80″ to seal against the stem 20 as it extends therethrough. Thevalve 80″ will function in a similar manner as a catheter or otherinstrument is passed through the valve 80″. In each case, which everinstrument is passed through the valve 80″, the bridge 84″ will slitonly enough to pass the particular device and will effectively create acustom passage sized just to the device passing through. As the dilator20 or other instrument is removed, the resiliency of the valve 80″ willcause the valve 80″ to substantially seal upon itself, with the concaveconfiguration of the conical portion 89″ assisting in such sealing.

Referring to FIGS. 22-24, the distal surface 94″ of the valve body 82″includes a pair of opposed arcuate grooves 96″. Each groove 96″ extendsslightly less than 180° such that the grooves 96″ are separated byopposed non-grooved portions 95″ of the distal surface 94″. Thenon-grooved portions 95″ are preferably co-planar with the slot 83″. Thegrooves 96″ in conjunction with the non-grooved portions 95″ provide aresilient hinge effect for the valve 80″. As an instrument or the likeis passed through the valve 80″, the central portion of the valve body82″ will begin to deflect distally over an arcuate path as indicated byarrows A in FIG. 22. The grooves 96″ provide space for the proximateportions 97″ of the distal surface 94″ to move during such deflection toallow easier passage, while the non-grooved portions 95″ provide somerigidity and assist in restoring the valve central portion to itoriginal position as the instrument is removed.

Referring to FIGS. 25 and 26, an exemplary cap member 100 will bedescribed. The sheath assembly 40 preferably uses two cap members 100which are identical, however, paired cap members having different butcomplimentary configurations may be utilized. Each cap member 100 of theexemplary embodiment includes a semi-circular platform 102 with adepending semi-circular wall 104 along its outer circumference. Theinside diameter of the wall 104 is approximately equal to our slightlylarger than the outside diameter of the sheath hub wall 58. A pair ofretaining openings 106 are defined through the circular wall 104, witheach retaining opening 106 positioned and configured to receive andretain a respective retaining tab 57 of the sheath hub 50. While twoopenings 106 and two corresponding tabs 57 are described herein, more orfewer connections may be utilized. A portion of the wall 104 oppositethe flat side 101 of the platform 102 defines a recess 105 which isconfigured to align with and receive a portion of a respective wingedtab 70 when the cap member 100 is connected to the hub body 52. Each endof the semi-circular wall 104 has a returning wall portion 108 whichextends radially inward and is configured to be received in a respectivenotch 54 of the hub body 52 when the cap member 100 is secured to thehub body 52. A semi-circular retaining ridge 116 depends from the distalsurface of the platform 102 and is co-axial with the platform 102. Thefunction of the ridge 116 will be described below.

A semi-circular opening 103 is defined through and co-axially with theplatform 102 such that the open side of the opening 103 is along theflat side 101 of the platform. A proximally extending semi-circular wall110 extends from the proximal side of the platform 102 about the opening103, and defines an open passage 111. In the illustrated embodiment, theplatform 101 extends radially inward of the wall 110 such that adiameter of the open passage 111 is slightly larger than the opening103. However, the platform 101 may terminate at the wall 110 such thatthe open passage 111 and the opening 103 have substantially the samediameter. The outside surface of the wall 110 has a diameter WD. Thediameter WD is approximately equal to or slightly smaller than thedistance E between the engagement portions 34 of the dilator hub 22.

As seen in FIGS. 27-29, when the cap members 100 are secured to the hubbody 52 opposite one another, the two semi-circular openings 103 and thetwo semi-circular walls 110 define a substantially circular openingwhich forms a part of the through passage 42. The diameter of theopening 103 and the open passage 111 may be sized to correspond to aparticular sheath or dilator size or a group of sizes within a givenrange. The ends of the wall 110 preferably have notches 112 on theproximal surface which when assembled define a stop receptacle 120 aswill be described below.

The portion of the wall 110 opposite the flat side 101 of the platform102 defines a radially outwardly extending proximal flange 114 which islongitudinally spaced from the platform 102 and extends beyond alongitudinal portion 117 of the wall 110 such that a receiving opening115 is defined between the flange 114 and the platform 102. The distancefrom the flat side 101 of the platform 102 to the longitudinal portion117 of the wall 110 is approximately one-half the diameter WD and thedistance from the flat side 101 to the radial edge of the flange 114 isapproximately one-half the distance F that the dilator hub extensions 33are spaced. As such, when the cap members 100 are connected to the hubbody 52, the wall 110 and portions 117 will define a diameter equal toWD which is approximately equal to or slightly smaller than the distanceE between the engagement portions 34 of the dilator hub 22 and theflanges 114 will define a distance approximately equal to or slightlylarger than the distance F that the dilator hub extensions 33 arespaced. The wall 110 and flanges 114 thereby define the locking portion129 of the sheath assembly 40.

Having described the components of the sheath hub 50, assembly thereofwill be described with reference to FIGS. 2 and 27-30. While assembly isdescribed with reference to the valve 80, it is appreciated that thevalve 80′ may be utilized in the same manner. It is noted that thesheath body 44 is not illustrated in FIGS. 27-30, but typically thesheath body 44 will be attached to the hub body 52 prior to finalassembly of the sheath hub 50. The valve 80 is positioned on the valveseat 60 within the hub body wall 58. As the valve 80 is positioned, thealignment posts 64 are received within the alignment openings 98 (seeFIG. 30) and the sheath hub wall 58 radially compresses the valve body82 such that the width of the slot 83 is reduced. As explained above,the posts 64 and openings 98 are arranged such that the valve 80 canonly be properly positioned in the desired orientation, i.e. with theproximal surface 86 facing proximally and the slot 83 aligned with thespace between the two cap members 100 and with the hub notches 54. Withthe valve 80 positioned on the seat 60, the distal surface 94 of thevalve body 82 seats upon the seat planar surface 62. The distal surface94 is spaced from the surface of groove 63. This space allows forcompression of the valve body 82 when the cap members 100 are secured,thereby enhancing the seal between the distal surface 94 and the planarsurface 62. The distal grooves 96 are positioned radially inward fromthe planar surface 62, aligned with the through passage 42, tofacilitate hinging of the central portion of the valve body 82.

Once the valve 80 is positioned, each cap member 100 is connected to arespective valve body halve 52 a, 52 b. The cap member 100 is snappedonto the valve body 52, with respective retaining tabs 57 received inthe retaining openings 106 as the wall 104 extends about the hub wall58. The platforms 102 preferably slightly compress the valve body 82when the cap members 100 are connected. Each cap member 100 ispreferably separably connectable such that interconnection between thetwo cap members 100 is not required to maintain the cap members 100 inposition. The cap members 100 are separated from one another by a slotwhich aligns with the notches 54. With the cap members 100 in place, theopenings 103 and 111 are co-axial with the tapered portion 89 and bore90 of the valve 80. The retaining ridges 116 are received in thecorresponding grooves 88 on the proximal surface 86 of the valve body82. The ridges 116 retain the out perimeter of the valve body 82 secureand enhance the seal on seat planar surface 62 while allowing thecentral portion of the valve body 82, radially inward of the grooves 88,to hingedly flex during insertion of an instrument. As shown in FIG. 29,the opposed notches 112 of adjacent cap members 100 define a stopreceptacle 120.

With the sheath hub 50 assembled, the dilator 20 may be inserted thereinand locked in place by engagement of the locking portions 39, 129 asdescribed with reference to FIGS. 31-33. Referring to FIG. 31, thedilator stem 36 is passed through the opening 111 defined by the capmembers 100 and then through the valve 80 (not shown in FIG. 31) andinto the sheath body 44. During insertion, the dilator 20 is orientedsuch that the dilator hub platform 32 is transverse to the direction ofthe flanges 114 of the cap members 100. With this orientation, thedilator stem 36 may be fully inserted with the cap member walls 110received between the engagement portions 34 of the dilator hub 22 asshown in FIG. 32. The engagement portions 34 contact the cap memberplatforms 102 upon full insertion.

After the dilator 20 has been fully inserted relative to the sheathassembly 40, the dilator hub 22 is rotated, as indicated by arrow B inFIG. 33, to the locking position. As the dilator hub 22 is rotated, thecap member flanges 114 are received in the locking grooves 45 of thedilator hub 22 and the engagement portions 34 are received in thereceiving openings 115. The cap member wall portions 117 are eachtapered at one end to facilitate passage of the engagement portions 34into the receiving openings 115 while the opposite ends of the wallportions 117 define a stop 121 which prevent over rotation of thedilator hub 22 relative to the sheath hub 50. Rotation from the initialfully inserted position to the locked position illustrated in FIG. 33 ispreferably over approximately 90°. As the dilator hub 22 reaches thelocked position, the stop members 25 are received in the stop receptacle120 such that a disengaging rotation force is necessary to unlock thedilator hub 22 relative to the sheath hub 50. Engagement of the lockingportions 39 and 129 prevents longitudinal movement between the dilator20 and the sheath assembly 40. The dilator and sheath assembly 10 is nowready for use as illustrated in FIG. 1.

These and other advantages of the present invention will be apparent tothose skilled in the art from the foregoing specification. Accordingly,it will be recognized by those skilled in the art that changes ormodifications may be made to the above-described embodiments withoutdeparting from the broad inventive concepts of the invention. It shouldtherefore be understood that this invention is not limited to theparticular embodiments described herein, but is intended to include allchanges and modifications that are within the scope and spirit of theinvention as defined in the claims.

What is claimed is:
 1. A valve for sealing the hub of a sheath assembly,the valve comprising a valve body with a bisecting slot extending into aproximal surface of the valve body and terminating at a depth less thanthe thickness of the valve body such that the remaining portion of thevalve body distally of the slot defines a bridge extending betweenopposed halves of the valve body such that a distal surface of the valvebody is substantially continuous.
 2. The valve according to claim 1wherein a central portion of the proximal surface of the valve body isconcave.
 3. The valve according to claim 2 wherein the valve bodyincludes a groove in the distal surface extending about the centralportion.
 4. The valve according to claim 2 wherein a portion of thedistal surface of the valve body opposite the concave proximal portionis convex.
 5. The valve according to claim 1 wherein a sealing slitextends through the valve body from the proximal surface of the valvebody to the distal surface of the valve body.
 6. The valve according toclaim 5 wherein the sealing slit extends at an angle between 45° to 135°relative to the bisecting slot.
 7. The valve according to claim 6wherein the sealing slit extends at an angle of approximately 90°relative to the bisecting slot.
 8. The valve according to claim 5wherein the sealing slit extends at an angle between 20° to 70° relativeto a longitudinal axis of the valve body.
 9. The valve according toclaim 8 wherein the sealing slit extends at an angle of approximately45° relative to the longitudinal axis of the valve body.
 10. The valveaccording to claim 8 wherein a proximal opening of the sealing slit ison one side of the longitudinal axis and a distal exit of the sealingslit is on an opposite side of the longitudinal axis.
 11. The valveaccording to claim 1 wherein the valve body includes a plurality of postreceiving apertures extending into the distal surface of the body. 12.The valve according to claim 10 wherein the post receiving apertures arein a non-symmetrical pattern relative to at least one axis of the valvebody.
 13. The valve according to claim 11 wherein the post receivingapertures are in a non-symmetrical pattern relative to each axis of thevalve body.
 14. A sheath assembly comprising: an elongated hollow sheathbody having a proximal body end, a distal body end, and a longitudinalaxis extending between the proximal body end and the distal body end; asheath hub fixedly connected to the proximal body end, the sheath hubhaving a hub proximal end and a hub distal end and defining a throughpassage extending from the hub distal end to the hub proximal end and incommunication with the hollow sheath body, the sheath hub furtherdefining a valve seat in proximity to the hub proximal end; a valveaccording to claim 1 seated in the valve seat and extending across andsealing the through passage; and one or more cap members secured to thesheath hub proximal end such that the valve is retained in the valveseat.
 15. The sheath assembly of claim 14, wherein the sheath bodyincludes at least one tear seam extending in a plane between theproximal body end and the distal body end and the sheath hub includes atleast one longitudinal notch, and wherein the at least one tear seam,the at least one longitudinal notch and the bisecting slot areco-planar.
 16. The sheath assembly of claim 14 wherein the one or morecap members define a depending skirt configured to receive a proximalportion of the sheath hub therein and wherein the skirt and hub haveinterlocking tabs and recesses to secure the one or more cap members tothe hub.
 17. The sheath assembly of claim 14 wherein the valve includesa groove in the proximal surface of the valve body and a portion of theone or more cap members is received in the groove.
 18. A dilator andsheath assembly comprising: a dilator including an elongated dilatorstem having a proximal dilator end and a dilator hub fixedly connectedto the proximal dilator end, wherein the dilator hub includes a lockingportion at a distal portion thereof; and a sheath assembly according toclaim 14 wherein the at least one cap member defines a mating lockingportion such that the locking portion of the dilator hub and the matinglocking portion of the cap provide a releasably locking engagementbetween the dilator and the sheath.
 19. The dilator and sheath assemblyof claim 18 wherein the locking portion of the dilator hub and themating locking portion of the cap are rotated between the lockingengagement and a non-locking engagement.
 20. The dilator and sheathassembly of claim 19 wherein the locking portion of the dilator hub andthe mating locking portion of the cap have a ramped engagementtherebetween.